Join a leading organization in the pharmaceutical sector where your expertise will enhance product development initiatives. Our client is seeking a dedicated professional to ensure compliance and quality standards are met in a challenging and impactful environment.As an ideal candidate, you are a skilledcompliance engineerwith a strong background in automation or data integrity. Your attention to detail and commitment to quality will be essential in this role.You execute qualification activities for all equipment in the plants, ensuring standards are upheld.You are the specialist owner of qualifications in multidisciplinary projects.You develop, execute, and report on qualification protocols that comply with GMP guidelines.You write URS, manage risk assessments, and create various qualification protocols (PQP, DQ, IQ, OQ, PQ).You conduct functional tests and create reports based on your findings during fieldwork.You document quality incidents, deviations, and follow up on corrective actions as per protocols.You participate in continuous improvement initiatives and manage CAPAs within the system.What are we looking for?You hold a Master's degree in a technical field or equivalent experience.You have 5-10 years of experience in qualification activities within the pharmaceutical sector.You are experienced in writing qualification documentation and executing protocols.You have a good understanding of GMP and GDP regulations.You possess knowledge of safety documentation related to change control as a plus.You demonstrate strong problem-solving and analytical skills.You work independently and in a planned manner.You are fluent in Dutch and English, both spoken and written.You have a solid command of Microsoft Office applications (Excel, Word).